نتایج جستجو برای: mnng
تعداد نتایج: 372 فیلتر نتایج به سال:
Fish/Radiosensitivity/Colony formation/Mutagens The sensitivities of three goldfish-cell lines to the lethal effects of four carcinogens/mutagens; 4-nitro quinoline-1-oxide (4NQO), 1-methyl-3-nitro-l-nitrosoguanidine (MNNG), mitomycin C (MMC) and bleo mycin (BLM), were compared using colony-formation assay. RBCF-1 and CAF-MM1 cells were more sensitive to 4NQO, BLM and UV than were GEM 199 cells...
In the presented paper, autofluorescent reporter of Escherichia coli K-12 recA::gfpmut2 strain, which contained a plasmid-borne transcriptional fusion between DNA-damage inducible recA promoter involved in the SOS regulon response and fast folding GFP variant reporter gene-gfpmut2, have been used. GFP-based bacterial biosensors allowed the detection of bacterial cells response to selected teste...
The induction of adenocarcinomas in the glandular stomach of the adult male Wistar rat by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) was used as a model to study the expression of the growth promoting peptide, transforming growth factor alpha (TGF alpha), during experimental gastric carcinogenesis. TGF alpha was identified using the monoclonal antibody Ab-2 and standard immunohistochemistry, t...
Topoisomerase I-directed agents are now in Phase I and II clinical trials and show great promise as potentially important agents for cancer chemotherapy. Because of their mechanism of action they may also be potential mutagens; however, their mutagenicity and oncogenicity still remain to be elucidated. We have previously shown that VP-16, a topoisomerase II-directed agent, induces sister chroma...
Background: Overexpression of cyclooxygenase 2 (COX-2) is frequently detected in gastric cancer and is believed to play a crucial role in gastric carcinogenesis. Aim: We examined the chemopreventive effect of a COX-2 inhibitor in an animal model of stomach carcinogenesis. Methods: Eighty six male Wistar rats were divided into six different treatment groups: group A, water alone (n = 5); group B...
Antimutagenic activity of a novel ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate.
A novel amphiphilic vitamin C derivative, disodium isostearyl 2-O-L-ascorbyl phosphate (VCP-IS-2Na) possessing an alkyl chain of C(18) to a stable ascorbate derivative sodium L-ascorbic acid 2-phosphate (VCP-Na), was synthesized and evaluated as an anti-mutagen with suppressive effect on SOS-inducing activity on mutagen in the Salmonella typhimurium TA1535/pSK1002 umu test. VCP-IS-2Na was assay...
Increased activity, membrane association, and secretion of cathepsin B have been shown to correlate positively with invasiveness and the metastatic properties of many tumor entities. Cathepsin B is able to directly facilitate invasion by degrading extracellular matrix components or to indirectly facilitate invasion by activating other matrix-degrading proteases like the urokinase-type plasminog...
PURPOSE The multikinase inhibitor sorafenib displays antitumor activity in preclinical models of osteosarcoma. However, in sorafenib-treated patients with metastatic-relapsed osteosarcoma, disease stabilization and tumor shrinkage were short-lived and drug resistance occurred. We explored the sorafenib treatment escape mechanisms to overcome their drawbacks. EXPERIMENTAL DESIGN Immunoprecipit...
BACKGROUND Overexpression of cyclooxygenase 2 (COX-2) is frequently detected in gastric cancer and is believed to play a crucial role in gastric carcinogenesis. AIM We examined the chemopreventive effect of a COX-2 inhibitor in an animal model of stomach carcinogenesis. METHODS Eighty six male Wistar rats were divided into six different treatment groups: group A, water alone (n = 5); group ...
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